Replication Catastrophe: When a Checkpoint Fails because of Exhaustion

被引:160
作者
Toledo, Luis [1 ,2 ]
Neelsen, Kai John [1 ]
Lukas, Jiri [1 ]
机构
[1] Univ Copenhagen, Novo Nordisk Fdn Ctr Prot Res, Fac Hlth & Med Sci, Blegdamsvej 3, DK-2200 Copenhagen, Denmark
[2] Univ Copenhagen, Fac Hlth & Med Sci, Dept Cellular & Mol Med, Ctr Chromosome Stabil, Blegdamsvej 3, DK-2200 Copenhagen, Denmark
基金
欧洲研究理事会;
关键词
DNA-DAMAGE RESPONSE; SINGLE-STRANDED-DNA; MINICHROMOSOME MAINTENANCE PROTEINS; ATR-DEPENDENT PHOSPHORYLATION; TOUSLED-LIKE KINASES; CELL-CYCLE; HOMOLOGOUS RECOMBINATION; CHK1; INHIBITION; BINDING-PROTEIN; FORK COLLAPSE;
D O I
10.1016/j.molcel.2017.05.001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Proliferating cells rely on the so-called DNA replication checkpoint to ensure orderly completion of genome duplication, and its malfunction may lead to catastrophic genome disruption, including unscheduled firing of replication origins, stalling and collapse of replication forks, massive DNA breakage, and, ultimately, cell death. Despite many years of intensive research into the molecular underpinnings of the eukaryotic replication checkpoint, the mechanisms underlying the dismal consequences of its failure remain enigmatic. A recent development offers a unifying model in which the replication checkpoint guards against global exhaustion of rate-limiting replication regulators. Here we discuss how such a mechanism can prevent catastrophic genome disruption and suggest how to harness this knowledge to advance therapeutic strategies to eliminate cancer cells that inherently proliferate under increased DNA replication stress.
引用
收藏
页码:735 / 749
页数:15
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